Simultaneous determination of beauvericin, enniatins, and fusaproliferin by high performance liquid chromatography

A rapid, sensitive and inexpensive HPLC method for routine screening of beauvericin, fusaproliferin, and enniatin B(1), A(1), and B has been optimized. Detection limits were determined, ranging between 0. 5 and 3.6 ng according to the compound obtained after spiking samples with each mycotoxin at 10-56 microg/mL concentration range; recoveries averaging from 56 to 74% were obtained. LC-MS conditions for enniatin analyses by API electrospray technique were set up, this allowing a unique identification of three different enniatins.     

Interaction of fusarium mycotoxins, fusaproliferin and fumonisin B1, with DNA studied by electrospray ionization mass spectrometry

Electrospray ionization mass spectrometry (ESI-MS) in negative ion mode was used to monitor the possible noncovalent adduct formations between DNA analogue oligonucleotides and two Fusarium mycotoxins, fumonisin B1 and fusaproliferin. Using mild experimental ESI conditions specific noncovalent interactions were detected between both single- and double-stranded model oligonucleotides and fusaproliferin with 1:1 stoichiometry. Similar association complexes were observed for the deacetyl derivative of fusaproliferin. There were no peaks due to adduct formation present in the mass spectra of fumonisin B1, incubated with oligonucleotides in a wide concentration range, suggesting no specific interaction for this molecule. In a competitive complexation reaction, another mycotoxin, the beauvericin, forms more stable association complex with DNA than fusaproliferin. These findings can be of use in the understanding of molecular mechanisms of action during apoptosis and can be correlated with the teratogenic effect of fusaproliferin.     

Molecular dynamics simulations on the mycotoxin fumonisin B1

The solution conformational properties of the mycotoxin fumonisin B(1) have been studied using molecular dynamics methodology. Fumonisins have been shown to inhibit sphinganine (sphingosine) N-acyltransferase (ceramide synthase) and show a wide range of toxic effects in many animals. This study of the solution properties of fumonisin B(1) attempts to add to the structural models necessary for the understanding of the binding and activity properties. The computational method uses a box with periodic boundaries, filled with explicit TIP3P water molecules, the substrate fumonisin B(1), and selected counterions for charge neutrality. The starting structure of fumonisin B(1) is added to the box by excluding water molecules. The explicit image method using 12-A cutoffs is applied to the system and molecular dynamics are carried out on different starting conformations at 300 K in 100-picosecond (ps) steps. Examination of the resulting equilibrated conformations suggests that the structure is relatively extended and that previous computational studies in vacuo, showing a compact folded structure, may not be consistent with the solution structure.     

Development of qualitative and semiquantitative immunoassay-based rapid strip tests for the detection of T-2 toxin in wheat and oat

Novel qualitative as well as semiquantitative rapid strip tests for screening of T-2 mycotoxin in agricultural commodities were developed. Colloidal gold particles were coated with monoclonal anti-T-2 antibodies and used as detector reagent, indicating the strip test results by formation of up to two colored lines in a competitive assay format. The test line comprises a protein conjugate of the T-2 mycotoxin and the control line an antispecies-specific antibody to confirm the correct test development. To perform the test, 5 g of sample was extracted in a ratio of 1:5 with methanol/water (70:30) by shaking for 3 min and the extract directly used without further cleanup steps. The T-2 toxin lateral flow device (LFD) presented has a cutoff level around 100 microg/kg for naturally contaminated wheat and oat. The semiquantitative test may be used in the lower micrograms per kilogram range and allows for rapid semiquantitative photometric classification of the level of sample contamination. For both tests, results were obtained within 4 min. The developed LFDs therefore allow for the first time fast and on-site screening for the determination of T-2 toxin in cereals.     

Production of a single-chain variable fragment antibody against fumonisin B1

The selection of synthetic antibody fragments from large phage libraries has become a common method for the generation of specific antibodies. The technique is particularly valuable when antibodies against small, non-immunogenic molecules (haptens) or highly toxic substances have to be produced. In addition, haptens are usually coupled to protein carriers, bearing the risk that the free hapten is not detectable. Here, a single variable chain antibody (scFv) against the highly toxic mycotoxin fumonisin B1 has been produced. The hapten was coupled via a linker to biotin. Using this conjugate and a naive scFv library, it was possible to circumvent both the necessity of immunization and the risk of a disguised hapten. The scFv obtained after three panning rounds was found to bind specifically to both free fumonisin B1 and fumonisin-biotin conjugate. Also fumonisin B2 was bound by the scFv. Modeling of both scFv and fumonisin B1 molecule revealed a good fitting of structures. The antibody obtained can potentially be used for developing a rapid and affordable immunoassay for detection of food contamination and can be applied in immunoaffinity chromatography, usually carried out prior to HPLC analysis of mycotoxin-contaminated food and feed.     

The development of immunoassays to identify and quantify species source of gum arabic

Gum arabic from Acacia senegal is commonly used as an additive in foodstuffs. Adulteration of gum arabic by other gums is a potential problem for reasons of safety and quality. This study aimed to develop and evaluate the use of enzyme-linked immunosorbent assays (ELISAs) for the detection of potential adulterants of gum arabic. Indirect competitive ELISAs (IC-ELISAs) were developed using the monoclonal antibodies SY CC7 (A. senegal), SY HH3 (Acacia seyal), and SY J1A1 (Combretum erythrophyllum). All IC-ELISAs had a working range of 0.005-10 mg/mL. The antibodies used were tested using the IC-ELISAs for cross-reactivity with other Acacia species and other gums. The antibodies were very specific for their respective antigens. Significant cross-reactivity was found for SY CC7 (between A. senegal and A. melliferae) and SY J1A1 (between C. erythrophyllum and A. seyal). The IC-ELISA was adapted further to test confectionery samples for the presence of gum arabic, which was successful, although recovery rates were reduced. Both IC- and plate trapped antigen ELISA (PTA-ELISA) formats were able to distinguish an adulterated sample of gum arabic when blended with either A. seyal or C. erythrophyllum. The PTA-ELISA was more sensitive for A. seyal than the IC-ELISA, but both were equally sensitive for C. erythrophyllum. The results suggest that the antibodies SY CC7, SY HH3, and SY J1A1 could be used in combination with each other for the detection of potential adulterants of A. senegal and the detection of gum arabic in foodstuffs.     

Immunochemical assays for direct sulfonamide antibiotic detection in milk and hair samples using antibody derivatized magnetic nanoparticles

Two direct enzyme-linked immunosorbent assays (ELISAs) have been developed for detection of sulfonamide antibiotic residues in milk samples. One of them is using magnetic nanoparticles (MNP) for target capture/enrichment (Ab-MNP-ELISA), and the second is performed using microtiter plates. Selective polyclonal antibodies, raised against 5-[6-(4-amino-benzenesulfonylamino)-pyridin-3-yl]-2-methyl-pentanoic acid (SA1), used in combination with an enzyme tracer prepared with the same hapten, has allowed us to reach a limit of detection (LOD) lower than 0.5 microg L(-1) for both ELISA formats. Sulfapyridine, sulfamethoxypyridazine, sulfathiazole, and sulfachloropyridazine are detected below the maximum residue limits established by the European Union for these antibiotics in milk (100 microg L(-1)). Matrix effects and accuracy studies performed with full-cream milk and hair extracts indicated a lack of interference from these sample matrices and very good recovery values, especially when using the Ab-MNP format. Milk samples and hair extracts can be measured without any previous treatment. The results demonstrate the high potential of these methods as screening tools for food safety and inspection controls.     

Characterization of the heat treatment undergone by milk using two inhibition ELISAs for quantification of native and heat denatured alpha-lactalbumin

Dairy industries are interested to know the heat treatment undergone by milk for controlling the quality of drinking milks or to control their heating systems. The purpose of this work was to develop a specific and sensitive technique for classification of the heat treatment a milk has been submitted to, without disposing of the original raw milk. For this purpose, alpha-lactalbumin was chosen as a bioindicator of heat treatment, and monoclonal antibodies specific for its native or heat-denatured form were raised and used in two inhibition ELISAs. ELISA allowed differentiation among raw, pasteurized, ultrahigh-temperature-treated, and sterilized milks without even having to know the alpha-lactalbumin concentration of the original raw milk. However, this technique was more suitable for intense heat treatments such as UHT treatment and sterilization because of the heat stability of alpha-lactalbumin.     

Analysis of zearalenone in cereal and Swine feed samples using an automated flow-through immunosensor

The development of a sensitive flow-though immunosensor for the analysis of the mycotoxin zearalenone in cereal samples is described. The sensor was completely automated and was based on a direct competitive immunosorbent assay and fluorescence detection. The mycotoxin competes with a horseradish-peroxidase-labeled derivative for the binding sites of a rabbit polyclonal antibody. Control pore glass covalently bound to Prot A was used for the oriented immobilization of the antibody-antigen immunocomplexes. The immunosensor shows an IC(50) value of 0.087 ng mL(-1) (RSD = 2.8%, n = 6) and a dynamic range from 0.019 to 0.422 ng mL(-1). The limit of detection (90% of blank signal) of 0.007 ng mL(-1) (RSD = 3.9%, n = 3) is lower than previously published methods. Corn, wheat, and swine feed samples have been analyzed with the device after extraction of the analyte using accelerated solvent extraction (ASE). The immunosensor has been validated using a corn certificate reference material and HPLC with fluorescence detection.     

Near-infrared spectroscopy analysis of seed coats of common beans ( Phaseolus vulgaris L.): a potential tool for breeding and quality evaluation

Near-infrared spectroscopy (NIRS) is a well-established technique for determining the components of foods. Sample preparation for NIRS is easy, making it suitable for breeding and/or quality evaluation, for which a large number of samples should be analyzed. We aimed to assess the feasibility of NIRS to estimate parameters that seem to influence consumers' perception of the seed coat of common beans: dietary fiber (DF), uronic acids (UA), ashes, calcium, and magnesium. We used reference methods to analyze ground seed coats of 90 common bean samples with a wide range of genetic variability and cultivated at many locations. We registered the NIR spectra on intact beans and ground seed coat samples. We derived partial least-squares (PLS) regression equations from a set of calibration samples and tested their predictive power in an external validation set. For intact beans, only RER values for ashes and calcium are good enough for very rough screening. For ground seed coat samples, the RPD and RER values for ashes (3.49 and 14.09, respectively) and calcium (3.57 and 12.70, respectively) are good enough for screening. RPD and RER values for DF (2.60 and 9.15, respectively) and RER values for magnesium (6.57) also enable rough screening. A poorer correlation was achieved for UA. We conclude that NIRS can help in common bean breeding research and quality evaluation.     

检测睾酮、孕酮、雌酮与雌三醇的双抗体酶免疫分析法

本文报道了自制的试剂建立了检测睾酮、孕酮、雌酮和雌三醇的双抗体酶免疫分析法。实验表明 ,这些测定具有很高灵敏度 (最小可测量为 0 1～ 1pg 孔 ) ,标准曲线范围为 0～ 40pg 孔 ;同相关类固醇激素 (孕酮、孕烯醇酮、睾酮、雄酮、雌酮、雌三醇和皮质酮等 )的交叉反应率一般在 0 1 %以下。测定的批内和批间变异系数分别在5 8%～ 7 2 %与 9 5%～ 1 0 5% (n =8)范围内。向血中添加激素标准品后的回收率在 94%～ 1 1 0 %范围内。用自制防腐剂处理后 ,液态抗体 (包括第二抗体 )、酶标记物和已包被第二抗体的滴定板可保持活性 5～ 1 2个月或更久 ( 4℃～ -2 0℃ )。此测定可节约激素特异抗体 4～ 1 0倍。初测人和动物的血、奶、尿样品表明所建立的 4种测定方法可分别用于人和动物体液中睾酮、孕酮、雌酮和雌三醇的定量检测     

Development of NIRS equations for food grain quality traits through exploitation of a core collection of cultivated sorghum

A sorghum core collection representing a wide range of genetic diversity and used in the framework of a sorghum breeding and genetics program was evaluated by near-infrared reflectance spectroscopy (NIRS) to predict food grain quality traits: amylose content (AM), protein content (PR), lipid content (LI), endosperm texture (ET), and hardness (HD). A total of 278 sorghum samples were scanned as whole and ground grain to develop calibration equations. Laboratory analyses were performed on NIRS sample subsets that preserved the core collection racial distribution. Principal component analysis performed on NIRS spectra evidenced a level of structure following known sorghum races, which underlined the importance of using a wide range of genetic diversity. Performances of calibration equations were evaluated by the coefficient of determination, bias, standard error of laboratory (SEL), and ratio of performance deviation (RPD). Ground grain spectra gave better calibration equations than whole grain. PR equation (RPD of 5.7) can be used for quality control. ET, LI, and HD equations (RPD of 2.9, 2.6, and 2.6, respectively) can be used for screening steps. Even with a small SEL in whole sample analysis, a RPD of 1.8 for AM confirmed that this variable is not easy to predict with NIRS.     

Assessment of the multi-mycotoxin-binding efficacy of a carbon/aluminosilicate-based product in an in vitro gastrointestinal model

A laboratory model, set to simulate the in vivo conditions of the porcine gastrointestinal tract, was used to study the small intestinal absorption of several mycotoxins and the effectiveness of Standard Q/FIS (a carbon/aluminosilicate-based product) in reducing mycotoxin absorption when added to multitoxin-contaminated diets. Mycotoxins were quickly absorbed in the proximal part of the small intestine at levels of 105 and 89% for fumonisins B1 and B2, respectively, 87% for ochratoxin A, 74% for deoxynivalenol, 44% for aflatoxin B1, and 25% for zearalenone. Addition of Standard Q/FIS to the diet (up to 2%, w/w) significantly reduced mycotoxin absorption, in a dose-dependent manner, up to 88% for aflatoxin B1, 44% for zearalenone, and 29% for the fumonisins and ochratoxin. Standard Q/FIS was ineffective in reducing deoxynivalenol uptake. These findings suggest that Standard Q/FIS can be used as a multitoxin adsorbent material to prevent the individual and combined adverse effects of mycotoxins in animals.     

The assessment of sediment screening risk in Venice Lagoon and other coastal areas using international sediment quality guidelines

Background, Aims and Scope  A number of studies carried out in recent years have shown the presence of a wide range of contaminants in the Venice Lagoon. It is important to have a good understanding of the ecological quality of Venice Lagoon sediments, in order to: i) define and locate areas where a threat to the environment is present and therefore an intervention is needed (i.e. in situ assessment and management); and ii) define sustainable and environmentally correct ways of managing sediments which are to be dredged for navigational purposes or in relation to other interventions (i.e., ex situ management). Methods  To examine how various regional and international SQGs ‘classed’ screening risk in Venice Lagoon sediments, data on median contaminant levels in surface sediments in Venice Lagoon resulting from a literature review were compared to a range of local and international sediment quality guidelines (SQGs). Then data on sediment contaminant levels in various areas and sub-basins of Venice Lagoon (main Lagoon, Porto Marghera and Venice City Canals) and in other regional and international transitional and coastal ecosystems with various levels of human impact (urbanization and industrialization) were evaluated based upon a selected consensus-based SQG. Finally, screening sediment quality for all of Venice Lagoon was mapped and contoured, relative to this consensus-based SQG and briefly compared with direct toxicity measurement through a battery of bioassays. Results  SQGs allow the sediment areas to be put in terms of potential, or screening, risk. Although there were some differences depending upon which specific SQGs were applied, the Venice SQGs and other international SQGs provided the same general picture of screening risk in Venice Lagoon despite geographic differences. Venice Lagoon South has the lowest screening risk levels, Venice Lagoon Central/North has the highest (and is nearest to the Porto Marghera and Venice City Canals sites). Discussion  The Venice Lagoon sediments have hazard quotients on the low end of the range of moderately urbanized and industrialized sites and higher than background case studies reviewed. Hg levels in the Venice Lagoon were generally higher than equivalent sites, while other contaminants were either equivalent or lower. In Porto Marghera (PM) and Venice City Canals (VC), for many contaminants of interest, PM, and for some, VC sediments have the highest levels of any case study reviewed. Ranges are high, so in all cases, remedial or disposal decisions should be based upon site-specific (and preferably tiered) data. Conclusions  The use of hazard quotients makes it possible to compare screening risks due to different mixes of contaminants within and between sites, but results should be interpreted with caution. How these sites rank when compared to some of the other highly industrialized sites depends upon how data are synthesized and communicated. Actual risk must be evaluated using a weight of evidence (WOE) approach, as site-specific bioavailability and background levels will differ both regionally and internationally. Recommendations and Perspectives  Whilst there are subtle differences, the current Venice sediment classifications (A, B and C) ‘performed’ in a similar manner to SQGs in similar classes, suggesting that regions of Venice Lagoon would not be classified much differently if other SQGs such as TEL, ERL, PEL, ERM or AET were adopted. The Italian sediment quality objectives, on the other hand, are significantly more conservative than any other SQGs examined, with the exception of the Flemish Reference values. A number of European nations are considering criteria based upon contaminant levels in relatively pristine modern sites, or based upon derivations of historical (pre-anthropogenic) contaminant levels. When used as a standard, such an approach lacks discriminating power, designating almost all sediments within an urbanized or industrialized region as of concern, or even, in many cases, mandating action or prohibiting various management approaches in a large percentage of sediments. While generally based upon the laudable desire to return sites to unimpacted levels, there is a risk that overprotective criteria have the opposite effect: by designating too large a percentage of sediments as requiring management or control, limited resources may be improperly allocated. Which set of SQGs is most ‘appropriate’ for the Venice Lagoon sediments depends upon the questions being asked. However, the Venice classifications are currently being used as pass-fail criteria, without consideration of site-specific conditions. The fact that they performed similarly to SQGs in similar classes suggests that any work to develop more site-specific SQGs (with the same general decision classes) would probably not make much difference in how sediments were ultimately classified and managed unless the fundamental approach was changed from a pass-fail to a tiered and WOE approach integrated in a comprehensive decision framework. For Venice Lagoon, and for other regions, although SQGs should be developed with care, in a scientifically defensible and risk-based manner, an equally or more important issue to be addressed is their role in overall decision frameworks. ESS-Submission Editor: Dr. Marc Babut (marc.babut@cemagref.fr)     

Does no‐till farming induce water repellency to soils?

Soil water repellency (SWR) is an intrinsic and dynamic soil property that can influence soil hydrology and crop production. Although several land use systems have been shown to induce water repellency in soil, the specific effects of no‐till cropping on SWR are poorly understood. This article reviews the impacts of no‐till on SWR and identifies research needs. No‐till cropping generally induces 1.5 to 40 times more SWR than conventional tillage, depending on soil type. This may result from near‐surface accumulation of hydrophobic organic C compounds derived from crop residues, microbial activity and reduced soil disturbance. While large SWR may have adverse impacts on soil hydrology and crop production, the level of SWR under no‐till relative to conventional tillage may contribute to aggregate stabilization and intra‐aggregate C sequestration. More research is needed to discern the extent and relevance of no‐till induced SWR. This includes: (1) further assessment of SWR under different tillage systems across a wide range of soil textures and climates, (2) comparison of the various methods for measuring SWR over a range of water contents, (3) inclusion of SWR in routine soil analysis and its use as a parameter to evaluate management impacts, (4) assessment of the temporal and spatial changes in SWR under field conditions, (5) further assessment of the impacts of the small differences in SWR between no‐till and conventionally tilled soils on crop production, soil hydrology and soil C sequestration, and (6) development of models to predict SWR for different tillage systems and soils.     

An improved method for measurement of soil aggregate stability using laser granulometry applied at regional scale

Laboratory‐based aggregate stability (AS) tests should be applied to material wetted to a moisture content comparable with that of a field soil. We have improved our original laser granulometer (LG)‐based AS test published in this journal by including a pre‐wetting stage. Our method estimates disaggregation reduction (DR; µm) for a soil sample (1–2‐mm diameter aggregates). Soils with more stable aggregates have larger DR values. We apply the new technique to soils from 60 cultivated sites across eastern England, with ten samples from each of six different parent material (PM) types encompassing a wide range of soil organic carbon (SOC) concentrations (1.2–7.0%). There are large differences between the median DR values (rescaled to < 500 µm) for soils over the PM types, which when used as a predictor (in combination with SOC concentration) accounted for 53% of the variation in DR. There was no evidence for including an interaction term between PM class and SOC concentration for the prediction of DR. After applying the aggregate stability tests with the 60 regional soil samples, they were stored for 9 months and the tests were repeated, resulting in a small but statistically significant increase in DR for samples from some, but not all, PM types. We show how a palaeosol excavated from a site in southern England can be used as an aggregate reference material (RM) to monitor the reproducibility of our technique. It has been suggested that soil quality, measured by critical soil physical properties, may decline if the organic carbon concentration is less than a critical threshold. Our results show that, for aggregate stability, any such thresholds are specific to the PM.     

A rapid aflatoxin B1 ELISA: development and validation with reduced matrix effects for peanuts, corn, pistachio, and Soybeans

Among the competitive ELISAs for aflatoxins that have been described, few have been adequately validated for reduced matrix effects. Using an aflatoxin B(1) (AFB(1))-specific polyclonal antibody (produced from AFB(1)-oxime conjugated to bovine serum albumin (BSA)) and AFB(1)- and AFB(2)-enzyme conjugates, four direct competitive ELISAs based on 96-microwell plates (two standard assays and two rapid assays) were developed, paying special attention to producing a robust assay relatively free of interferences for a range of agricultural products. The antibody was AFB(1)-specific, detecting only AFB(1) in a mixture of four aflatoxins (AFB(1), AFB(2), AFG(1), and AFG(2)), but showed significant cross-reaction with AFG(1) (57-61%) when an individual compound was tested. Standard assays (long assays) exhibited higher sensitivities than rapid assays (short assays) with IC(50) values of 12 +/- 1.5 and 9 +/- 1.5 microg/kg in sample (with 1 in 5 dilution of sample extract) for AFB(1) and AFB(2)-enzyme conjugates, respectively. These assays have narrower detection ranges (7.1-55.5 microg/kg in sample) and required dilution of sample extracts to overcome solvent and matrix interferences, making these assays less ideal as analytical methods. Rapid assays exhibited IC(50) values of 21.6 +/- 2.7 and 12 microg/kg in sample for AFB(1)- and AFB(2)-enzyme conjugates, respectively. These assays have ideally broader detection ranges (4.2-99.9 microg/kg in sample) and showed no methanol effects up to 80% with significantly reduced matrix interferences as a result of the shorter incubation times and increasing the amounts of enzyme conjugate used. Therefore, the rapid assays were formatted to perform without a need for extract dilution. The rapid assays can be completed within 15 min, potentially suitable for receival bays where quick decision-making to segregate low and high contamination is critical. Further validation using the rapid assay with AFB(1)-enzyme conjugate indicated relatively good recoveries of AFB(1) spiked in corn, peanuts, pistachio, and soybeans, which were free from significant matrix effects. It can be concluded that this rapid assay would be suitable for monitoring aflatoxin AFB(1) at current legal maximum residue limits of 10 microg/kg in food such as corn, peanuts, pistachio, and soybeans.     

2010—2019年欧盟食品和饲料快速预警系统对华通报食品真菌毒素污染分析及应对策略

欧盟是世界第一大经济联合体,也是我国食品出口的主要市场之一。本文就 2010—2019年欧盟食品和饲料快速预警系统(RASFF)对我国食品通报信息进行统计分析和总结,重点分析了真菌毒素污染类食品通报近十年的发展变化趋势,发现真菌毒素污染在所有危害类型中排第一位,是我国食品出口欧盟的最大阻碍;进一步分析了欧盟RASFF对华通报食品真菌毒素污染数量居高不下的原因,并就如何减少相关通报提出了一些应对策略和建议。研究数据将为我国食品出口提供参考,为我国食品安全体系建设尤其是真菌毒素防控体系建设提供科学依据和重要借鉴。     

The application of biosensors to fresh produce and the wider food industry

The inherent specificity, selectivity, and adaptability of biosensors make them ideal candidates for use throughout the food industry. Potential applications within the supply chain range from testing of foodstuffs for maximum pesticide residue verification through to the routine analysis of analyte(s) concentrations, such as, glucose, sucrose, alcohol, etc., which may be indicators of food quality/acceptability. Biosensor formats include simple "one-shot" disposable devices that can be used either in the field or integrated into more sophisticated laboratory instruments. Until now, the main impact of these devices has been in the medical diagnostics field. However, with ongoing technical development, the food industry will be one of the prime beneficiaries of biosensor technology in the future. This report assesses the current and future trends in the application of biosensors to fresh produce and the wider food industry, focusing on both potential and current target analytes that are fundamental to fresh produce quality, traceability, and safety.     

Simultaneous extraction and fractionation and thin layer chromatographic determination of 14 mycotoxins in grains.

A simple, systematic analytical method for multiple mycotoxins was developed for detecting 14 mycotoxins; aflatoxins B1, B2, G1, and G2, sterigmatocystin, T-2 toxin, diacetoxyscirpenol, neosolaniol, fusarenon X, zearalenone, ochratoxin A, citrinin, luteoskyrin, and rugulosin. These mycotoxins were extracted with 20% H2SO4-4% KCl-acetonitrile (2 + 20 + 178), defatted with isooctane, and transferred to chloroform. The chloroform extract was cleaned up by silica gel column chromatography; the first 10 toxins were eluted with chloroform-methanol (97 + 3) and the remaining 4 toxins with benzene-acetone-acetic acid (75 + 20 + 5). Each fraction was analyzed by thin layer chromatography for the final determination. The method has been applied to polished rice, rough rice, corn, wheat, and peanuts as an analytical screening procedure. The detection limits in these commodities ranged from 10.00 to 800.0 microgram/kg, depending on the mycotoxin, but all limits were superior to those obtained for the individual mycotoxins by using other methods.